Evidence map›Paper›PMID 22228408›Full record

ArticlePlant molecular biology2012

A chloroplast-derived C4V3 polypeptide from the human immunodeficiency virus (HIV) is orally immunogenic in mice.

Néstor Rubio-Infante, Dania O Govea-Alonso, Ángel G Alpuche-Solís, Ana Lilia García-Hernández, Ruth E Soria-Guerra, L M Teresita Paz-Maldonado, Damaris Ilhuicatzi-Alvarado, Javier T Varona-Santos, Leticia Verdín-Terán, Schuyler S Korban and 2 more

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In one paragraph

Article in Plant molecular biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
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  7. Review
  8. Plants as Factories for Human Pharmaceuticals: Applications and Challenges.International journal of molecular sciences · 2015
    Review
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  10. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 2 countries.

Néstor Rubio-InfanteLaboratorio de Biofarmacéuticos Recombinantes, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 6, 78210 San Luis Potosí, Mexico.
Dania O Govea-Alonso
Ángel G Alpuche-Solís
Ana Lilia García-Hernández
Ruth E Soria-Guerra
L M Teresita Paz-Maldonado
Damaris Ilhuicatzi-Alvarado
Javier T Varona-Santos
Leticia Verdín-Terán
Schuyler S Korban
Leticia Moreno-Fierros
Sergio Rosales-Mendoza
Autonomous University of San Luis Potosí · MXAutonomous University of Tlaxcala · MXUniversidad Nacional Autónoma de México · MXInstitute for Scientific and Technological Research · MXUniversity of Illinois Urbana-Champaign · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the human immunodeficiency virus (HIV) causes one of the most important infectious diseases worldwide, attempts to develop an effective vaccine remain elusive. Designing recombinant proteins capable of eliciting significant and protective mammalian immune responses remain a priority. Moreover, large-scale production of proteins of interest at affordable cost remains a challenge for modern biotechnology. In this study, a synthetic gene encoding a C4V3 recombinant protein, known to induce systemic and mucosal immune responses in mammalian systems, has been introduced into tobacco chloroplasts to yield high levels of expression. Integration of the transgene into the tobacco plastome has been verified by Southern blot hybridization. The recombinant C4V3 protein is also detected in tobacco chloroplasts by confocal microscopy. Reactivity of the heterologous protein with both an anti-C4V3 rabbit serum as well as sera from HIV positive patients have been assayed using Western blots. When administered by the oral route in a four-weekly dose immunization scheme, the plant-derived C4V3 has elicited both systemic and mucosal antibody responses in BALB/c mice, as well as CD4+ T cell proliferation responses. These findings support the viability of using plant chloroplasts as biofactories for HIV candidate vaccines, and could serve as important vehicles for the development of a plant-based candidate vaccine against HIV.

Indexed as

Administration, OralAnimalsAnti-HIV AgentsChloroplastsFemaleHIV Envelope Protein gp120HIV SeropositivityHumansImmunity, MucosalImmunizationMiceMice, Inbred BALB CNicotianaPeptide FragmentsPeptidesPlants, Genetically ModifiedAnti-HIV AgentsHIV Envelope Protein gp120HIV envelope protein gp120 (305-321)Peptide FragmentsPeptidesRecombinant ProteinsVaccines, Synthetic

Identifiers

PMID22228408
OpenAlexW2013082873

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.